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Journal Abstract Search

263 related items for PubMed ID: 30504332

  • 1. Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia.
    King AJ, Higgs DR.
    Hematology Am Soc Hematol Educ Program; 2018 Nov 30; 2018(1):353-360. PubMed ID: 30504332
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  • 3. Hemoglobin Bart's hydrops fetalis: charting the past and envisioning the future.
    Amid A, Liu S, Babbs C, Higgs DR.
    Blood; 2024 Aug 22; 144(8):822-833. PubMed ID: 38457773
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  • 4. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
    Wang W, Yap CH, Loh SF, Tan AS, Lim MN, Prasath EB, Chan ML, Tan WC, Jiang B, Yeo GH, Mathew J, Ho A, Ho SS, Wong PC, Choolani MA, Chong SS.
    Reprod Biomed Online; 2010 Nov 22; 21(5):642-8. PubMed ID: 20864413
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  • 6. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 Nov 22; 121(4):227-33. PubMed ID: 19546525
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    Motiani A, Zubair M, Sonagra AD.
    ; 2024 01 22. PubMed ID: 36508547
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  • 8. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Kunyanone N, Sittiprasert S, Thungkham K, Junorse S, Pongsawatkul K, Pattanaporn W, Jitwong C, Sanguansermsri T.
    J Med Assoc Thai; 2010 Nov 22; 93(11):1243-8. PubMed ID: 21114201
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  • 9. Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chain.
    Tatu T, Kiewkarnkha T, Khuntarak S, Khamrin S, Suwannasin S, Kasinrerk W.
    Int J Hematol; 2012 Apr 22; 95(4):386-93. PubMed ID: 22438184
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  • 10. An increase of the cardiothoracic ratio leads to a diagnosis of Bart's hydrops.
    Phupong V.
    J Med Assoc Thai; 2006 Apr 22; 89(4):509-12. PubMed ID: 16696397
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  • 13. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.
    Am J Hematol; 1985 Mar 22; 18(3):289-96. PubMed ID: 2983536
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  • 14. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007 Mar 22; 22(4):264-8. PubMed ID: 17369692
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  • 16. Invasive prenatal diagnosis of α-thalassemia to control Hb Bart's hydrops fetalis syndrome: 15 years of experience.
    Lai K, Li S, Lin W, Yang D, Chen W, Li M, Pang L, Chen P.
    Arch Gynecol Obstet; 2018 Aug 22; 298(2):307-311. PubMed ID: 29948167
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  • 18. Universal newborn screening for Hb H disease in California.
    Lorey F, Cunningham G, Vichinsky EP, Lubin BH, Witkowska HE, Matsunaga A, Azimi M, Sherwin J, Eastman J, Farina F, Waye JS, Chui DH.
    Genet Test; 2001 Aug 22; 5(2):93-100. PubMed ID: 11551109
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  • 19. Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.
    Chang JG, Chen CP, Ho HJ, Lin CP, Lee LS, Chen PH.
    Int J Hematol; 1992 Oct 22; 56(2):155-9. PubMed ID: 1421177
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  • 20. Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (- -SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.
    Jomoui W, Tepakhan W, Karnpean R.
    Hemoglobin; 2019 Oct 22; 43(4-5):236-240. PubMed ID: 31635494
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